| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156701 | BAA02g04650 | A02 | 2021473 | G | A | upstream_gene_variant | MODIFIER | c.-3180C>T| |
S173 |
| 156702 | BAA02g04650 | A02 | 2021495 | G | A | upstream_gene_variant | MODIFIER | c.-3202C>T| |
S184 |
| 156703 | BAA02g04650 | A02 | 2022950 | G | A | upstream_gene_variant | MODIFIER | c.-4657C>T| |
S256 |
| 156704 | BAA02g04670 | A02 | 2024555 | G | A | upstream_gene_variant | MODIFIER | c.-4240G>A| |
S48 |
| 156705 | BAA02g04670 | A02 | 2025320 | C | T | upstream_gene_variant | MODIFIER | c.-3475C>T| |
S216 |
| 156706 | BAA02g04660 | A02 | 2026177 | C | T | missense_variant | MODERATE | c.955G>A|p.Val319Met |
S207 |
| 156707 | BAA02g04660 | A02 | 2026920 | C | T | missense_variant | MODERATE | c.212G>A|p.Ser71Asn |
S289 S290 |
| 156708 | BAA02g04660 | A02 | 2027132 | C | T | upstream_gene_variant | MODIFIER | c.-1G>A| |
S287 |
| 156709 | BAA02g04660 | A02 | 2027824 | G | A | upstream_gene_variant | MODIFIER | c.-693C>T| |
S261 |
| 156710 | BAA02g04670 | A02 | 2029706 | C | T | synonymous_variant | LOW | c.561C>T|p.Phe187Phe |
S66 |
| 156711 | BAA02g04670 | A02 | 2029895 | C | T | synonymous_variant | LOW | c.633C>T|p.Leu211Leu |
S46 |
| 156712 | BAA02g04670 | A02 | 2030255 | G | A | missense_variant | MODERATE | c.752G>A|p.Arg251Lys |
S125 |
| 156713 | BAA02g04660 | A02 | 2030484 | C | T | upstream_gene_variant | MODIFIER | c.-3353G>A| |
S144 |
| 156714 | BAA02g04670 | A02 | 2031136 | C | T | missense_variant | MODERATE | c.1121C>T|p.Ser374Phe |
S54 |
| 156715 | BAA02g04680 | A02 | 2032065 | C | T | missense_variant | MODERATE | c.298G>A|p.Asp100Asn |
S178 |
| 156716 | BAA02g04680 | A02 | 2032493 | C | T | upstream_gene_variant | MODIFIER | c.-60G>A| |
S55 |
| 156717 | BAA02g04680 | A02 | 2032862 | C | T | upstream_gene_variant | MODIFIER | c.-429G>A| |
S301 S304 |
| 156718 | BAA02g04680 | A02 | 2033199 | G | A | upstream_gene_variant | MODIFIER | c.-766C>T| |
S78 |
| 156719 | BAA02g04690 | A02 | 2033854 | C | T | missense_variant | MODERATE | c.350C>T|p.Ala117Val |
S181 |
| 156720 | BAA02g04690 | A02 | 2033944 | C | T | missense_variant | MODERATE | c.440C>T|p.Ser147Phe |
S111 |
| 156721 | BAA02g04680 | A02 | 2034352 | G | A | upstream_gene_variant | MODIFIER | c.-1919C>T| |
S228 |
| 156722 | BAA02g04680 | A02 | 2034578 | C | T | upstream_gene_variant | MODIFIER | c.-2145G>A| |
S255 |
| 156723 | BAA02g04680 | A02 | 2034855 | C | T | upstream_gene_variant | MODIFIER | c.-2422G>A| |
S207 |
| 156724 | BAA02g04680 | A02 | 2035251 | C | T | upstream_gene_variant | MODIFIER | c.-2818G>A| |
S8 |
| 156725 | BAA02g04680 | A02 | 2035488 | G | A | upstream_gene_variant | MODIFIER | c.-3055C>T| |
S297 |